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https://www.selleckchem.com/products/brd0539.html satisfaction with anesthesia and are unreliable judges of patient comfort perioperatively. Contemporary monovision techniques use premium intraocular lenses (IOLs), either in both eyes or at least in the non-dominant one. Primary objective of this study was to compare the efficacy of premium monovision (implantation of the trifocal diffractive Panoptix IOL in the non-dominant eye and the bifocal hybrid refractive-diffractive Restor IOL in the dominant eye), against bilateral myopic monovision (implantation of the monofocal SN60WF IOL targeting -0.50 D in the dominant eye and -1.25 D myopia in the non-dominant one), hybrid monovision (implantation of Panoptix in the non-dominant eye and SN60WF in the dominant eye) and bilateral trifocal implantation (with bilateral Panoptix implantation). This is a prospective, comparative, clinic-based trial. Cataract patients populated four study groups Monovision Group (MoG), Multifocal Lens Group (MfG), Hybrid Monovision Group (HmG) and Premium Monovision Group (PmG). Binocular Uncorrected Distance Visual Acuity (UDVA), Uncorrected Reading Acuity and Criticacal techniques present satisfactory outcomes. Premium monovision seems to demonstrate the best outcomes. ClinicalTrials.gov, NCT04618380. Registered 05 November 2020, https//clinicaltrials.gov/ct2/show/NCT04618380. ClinicalTrials.gov, NCT04618380. Registered 05 November 2020, https//clinicaltrials.gov/ct2/show/NCT04618380. To compare the acquisition time necessary to obtain the optical biometry plus corneal power measurement using the IOLMaster 700 with central topography with that found using the standard IOLMaster 700 in combination with two corneal topographers, when acquiring biometry measurements during cataract evaluation. This prospective, observational, controlled study included 96 eyes of 96 cataract patients. Acquisition times were registered for different conditions time required for one complete measurement with IOL
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